Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:160030885-160031033 | Rare:49; Clinvar (benign):1 | ||||
chr1:160101124-160101329 | Common:1; Rare:38 | ||||
chr1:160124788-160125070 | Common:2; Rare:43 | ||||
chr1:160206111-160206274 | Rare:38 | ||||
chr1:160342398-160342650 | Common:2; Rare:54 | ||||
chr1:160652276-160652502 | Common:2; Rare:39 | ||||
chr1:160699551-160699848 | Common:5; Rare:72 | ||||
chr1:160726349-160726645 | Common:5; Rare:47 | ||||
chr1:160866351-160866443 | Rare:14 | ||||
chr1:160866839-160867117 | Common:4; Rare:52 | ||||
chr1:160875117-160875204 | Common:1; Rare:15 | ||||
chr1:160949192-160949372 | Common:2; Rare:33 | ||||
chr1:161013677-161014101 | Common:1; Rare:74 | ||||
chr1:161016729-161016754 | Rare:2 | ||||
chr1:161083345-161083827 | Common:1; Rare:86 |